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Journal Abstract Search

250 related items for PubMed ID: 9054190

  • 21.
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  • 22. NO message from muscle.
    Grozdanovic Z.
    Microsc Res Tech; 2001 Nov 01; 55(3):148-53. PubMed ID: 11747089
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  • 26. Relocalization of neuronal nitric oxide synthase (nNOS) as a marker for complete restoration of the dystrophin associated protein complex in skeletal muscle.
    Wells KE, Torelli S, Lu Q, Brown SC, Partridge T, Muntoni F, Wells DJ.
    Neuromuscul Disord; 2003 Jan 01; 13(1):21-31. PubMed ID: 12467729
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  • 27. Adhalin (alpha-sarcoglycan) is not required for anchoring of nitric oxide synthase I (NOS I) to the sarcolemma in non-mammalian skeletal (striated) muscle fibers.
    Gossrau R, Christova T, Grozdanovic Z, Blottner D.
    Acta Histochem; 1996 Jul 01; 98(3):345-55. PubMed ID: 8863863
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  • 29. Heme oxygenase-2 is present in the sarcolemma region of skeletal muscle fibers and is non-continuously co-localized with nitric oxide synthase-1.
    Baum O, Feussner M, Richter H, Gossrau R.
    Acta Histochem; 2000 Aug 01; 102(3):281-98. PubMed ID: 10990066
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  • 30. Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins.
    Tidball JG, Wehling-Henricks M.
    Mol Genet Metab; 2004 Aug 01; 82(4):312-20. PubMed ID: 15308129
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  • 31. Utility of dystrophin and utrophin staining in childhood muscular dystrophy.
    Sundaram C, Vydehi B, Meena K, Murthy J.
    Indian J Pathol Microbiol; 2004 Jul 01; 47(3):367-9. PubMed ID: 16295426
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  • 33. Expression of nitric oxide synthase immunoreactivity in the human female intramural striated urethral sphincter.
    Ho KM, Borja MC, Persson K, Brading AF, Andersson KE.
    J Urol; 2003 Jun 01; 169(6):2407-11. PubMed ID: 12771807
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  • 36. Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophin.
    Matsumura K, Tomé FM, Ionasescu V, Ervasti JM, Anderson RD, Romero NB, Simon D, Récan D, Kaplan JC, Fardeau M.
    J Clin Invest; 1993 Aug 01; 92(2):866-71. PubMed ID: 8349821
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  • 37. Association of soluble guanylate cyclase with the sarcolemma of mammalian skeletal muscle fibers.
    Feussner M, Richter H, Baum O, Gossrau R.
    Acta Histochem; 2001 Jul 01; 103(3):265-77. PubMed ID: 11482373
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  • 38. Animal models for muscular dystrophy show different patterns of sarcolemmal disruption.
    Straub V, Rafael JA, Chamberlain JS, Campbell KP.
    J Cell Biol; 1997 Oct 20; 139(2):375-85. PubMed ID: 9334342
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  • 39. Nitric oxide and l-arginine cause an accumulation of utrophin at the sarcolemma: a possible compensation for dystrophin loss in Duchenne muscular dystrophy.
    Chaubourt E, Fossier P, Baux G, Leprince C, Israël M, De La Porte S.
    Neurobiol Dis; 1999 Dec 20; 6(6):499-507. PubMed ID: 10600405
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  • 40. Vasomodulation by skeletal muscle-derived nitric oxide requires alpha-syntrophin-mediated sarcolemmal localization of neuronal Nitric oxide synthase.
    Thomas GD, Shaul PW, Yuhanna IS, Froehner SC, Adams ME.
    Circ Res; 2003 Mar 21; 92(5):554-60. PubMed ID: 12600881
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